Methylprednisolone Sodium Succinate Injection
Product Images NDC 43598-128

9 FDA label images from Dr. Reddy's Laboratories Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Sodium Succinate (NDC 43598-128). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Carton1 (Carton1)

Carton1 (Carton1)
Packaging label for Methylprednisolone Sodium Succinate injection, USP 40 mg per vial by Dr. Reddy's Laboratories Inc. Intended for intramuscular or intravenous use only, this label specifies a single-dose vial with instructions to discard any unused portion. The label includes dosage strength, lot/expiration fields, and cautions about the absence of diluent and use of preservatives.*
FDA Label Image

Carton2 (Carton2)

Carton2 (Carton2)
Packaging label for Methylprednisolone Sodium Succinate Injection, USP 125 mg per vial, supplied as a single-dose vial for intramuscular or intravenous use. The label includes instructions to discard unused portions and notes manufacturer as Dr. Reddy's Laboratories Inc. The label also specifies the product is Rx only and provides product NDC information.*
FDA Label Image

Carton3 (Carton3)

Carton3 (Carton3)
Methylprednisolone sodium succinate 500 mg per vial injection label by Dr. Reddy's Laboratories Inc. The label is for a multi-dose vial intended for intramuscular or intravenous use. It includes storage instructions, recommended reconstitution with benzyl alcohol, and warnings that the package does not contain diluent. The label shows the NDC 43598-128-11 and detailed usage and dosage information.*
FDA Label Image

Carton4 (Carton4)

Carton4 (Carton4)
Packaging label for methylPREDNISolone Sodium Succinate for Injection, USP 1 g per vial, an injectable drug by Dr. Reddy's Laboratories Inc. The label states it is for intramuscular or intravenous use only, multi-dose vial. It includes storage instructions, dosage information, bar code, lot and expiration data area, and warnings in black, green, and red text on a white background.*
FDA Label Image

Container1 (Container1)

Container1 (Container1)
Label for Methylprednisolone Sodium Succinate for Injection, USP, 40 mg per vial. It is a single dose vial intended for intramuscular or intravenous use, with instructions to discard the unused portion. The label notes reconstitution instructions, manufacturer Tianjin Kingyork Pharmaceuticals Co., Ltd. in China, and distribution by Dr. Reddy's Laboratories, Inc., Princeton, NJ, USA.*
FDA Label Image

Container2 (Container2)

Container2 (Container2)
Label for Methylprednisolone Sodium Succinate Injection, USP 125 mg per vial, for intramuscular or intravenous use. The single-dose vial requires reconstitution with 2 mL water for injection. Manufactured by Tianjin Kingyork Pharmaceuticals, distributed by Dr. Reddy's Laboratories Inc. Includes instructions to discard unused portion and protect from light.*
FDA Label Image

Container3 (Container3)

Container3 (Container3)
Label for Methylprednisolone Sodium Succinate Injection, USP 500 mg per vial, intended for intramuscular or intravenous use. It is a multi-dose vial labeled Rx only. The label notes no diluent included and recommends bacteriostatic water with benzyl alcohol as a diluent. It is manufactured by Tianjin Kingyork Pharmaceuticals and distributed by Dr. Reddy's Laboratories, Inc.*
FDA Label Image

Container4 (Container4)

Container4 (Container4)
Label for Methylprednisolone Sodium Succinate Injection, USP, 1 g per vial, for intramuscular or intravenous use only. The multi-dose vial is distributed by Dr. Reddy's Laboratories Inc. The label includes storage instructions to keep at 20° to 25°C and to protect from light. It states the package does not contain diluent and recommends using bacteriostatic water for injection with benzyl alcohol as a preservative. The vial is manufactured by Tianjin Kingyork Pharmaceuticals Co., Ltd. in China.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of methylprednisolone sodium succinate, showing its molecular framework with characteristic steroid rings and functional groups.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.